Regulatory Affairs Specialist: Clinical Trials & MA

IQVIA; Estado de México; Sur place; MXN 420 000 - 600 000; Plein temps

Résumé du poste

IQVIA is seeking a Regulatory Affairs professional to prepare and review regulatory submissions for clinical trials and marketing authorization activities. The role supports internal and external clients under general supervision, participating in project teams and client meetings as needed.

The candidate should have 2–3 years of regulatory affairs experience, a life sciences degree (BSc preferred), and fluent English.

Qualifications

• Bachelor's degree in life sciences completed.
• 2–3 years of regulatory affairs experience.
• Fluent English in writing, speaking and reading.
• Strong interpersonal communication and organizational skills.
• Experience with regulatory publishing and submission publishing activities.

Responsabilités

• Act as Regulatory Team Member on small, straightforward regulatory projects under supervision.
• Identify project needs, track timelines and manage day-to-day workload with senior staff.
• Prepare and/or review regulatory documentation in life sciences domains.
• Participate in project teams with internal and external customers and communicate confidently.
• Prepare slides/background material for small business development meetings and present to clients by phone or in person.
• May prepare and deliver trainings as appropriate.
• Perform other tasks delegated by Regulatory management.
• Make minor improvements to systems and processes to solve problems.

Connaissances

Fluent English

Interpersonal communication

Organization skills

Self-motivation

Formation

Bachelor's Degree in Life sciences

Master's Degree in Life sciences

Outils

Microsoft Office

Publishing tools

PDF Publishing

Description du poste

IQVIA is seeking a Regulatory Affairs professional to prepare and review regulatory submissions for clinical trials and marketing authorization activities. The role supports internal and external clients under general supervision, participating in project teams and client meetings as needed.

The candidate should have 2–3 years of regulatory affairs experience, a life sciences degree (BSc preferred), and fluent English.